Jerzmanowski A, Staroń K, Tyniec B, Toczko K
Biochim Biophys Acta. 1978 Dec 21;521(2):493-501. doi: 10.1016/0005-2787(78)90291-5.
Intercalation of ethidium bromide into DNA influences the rate of its digestion with micrococcal nuclease in opposite directions depending on whether it is free DNA or DNA in chromatin. In the case of free DNA the binding of ethidium bromide, starting from a very low concentration, results in the inhibition of the rate of digestion (increasing constantly with the increase of the ethidium bromide/nucleotide ratio). In contrast to free DNA the digestion rate as well as the overall amount of nuclease susceptible DNA is increased upon ethidium bromide binding to chromatin, with maximum enhancement around the saturation of intercalation sites. The saturation of intercalation sites in chromatin leads also to the disappearance of the typical micrococcal nuclease digestion pattern of DNA upon gel electrophoresis. Instead, a random cleavage pattern is observed. These data indicate that partial unwinding of chromatin DNA by ethidium bromide results in unmasking new sites for nuclease action. Interpretation of this finding in terms of the nucleosomal structure of chromatin and the mode of ethidium bromide binding to chromatin DNA indicates that newly unmasked sites are localized within the core particle DNA.
溴化乙锭嵌入DNA会对其被微球菌核酸酶消化的速率产生相反影响,这取决于DNA是游离状态还是染色质中的DNA。对于游离DNA,从极低浓度开始,溴化乙锭的结合就会导致消化速率受到抑制(随着溴化乙锭/核苷酸比率的增加而持续增加)。与游离DNA相反,当溴化乙锭与染色质结合时,核酸酶敏感DNA的消化速率以及总量都会增加,在嵌入位点饱和时增强最为明显。染色质中嵌入位点的饱和还会导致凝胶电泳时DNA典型的微球菌核酸酶消化模式消失。相反,会观察到随机切割模式。这些数据表明,溴化乙锭使染色质DNA部分解旋,从而暴露出核酸酶作用的新位点。从染色质的核小体结构以及溴化乙锭与染色质DNA的结合模式来看,这一发现表明新暴露的位点位于核心颗粒DNA内。